In contrast to the studies described above, Tuzun et al. 28 compared the human genome reference sequence with representative fragments of another genome using the fosmid paired-end sequence approach.

The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more ...

One in every 10 people worldwide is impacted by a rare genetic disease but about 50% of them remain undiagnosed despite rapid ...

Washington University School of Medicine in St. Louis has received two large grants renewing funding for the Human Pangenome ...

The Human Pangenome Refence Sequencing Project seeks to gather genomic sequences from a diverse representation of human participants. Two new grants from the NIH will support project contributions by ...

With 10K genomic data now publicly available, India takes a major leap in genetic research. In today’s 'Knowledge Nugget', ...

Bjarni V. Halldorsson and Kari Stefansson, scientists at deCODE genetics, discuss the paper: Complete recombination map of ...

Memorial Sloan Kettering Cancer Center researchers are helping to map the landscape of viruses that infect us all, and to ...

Scientists at deCODE genetics/Amgen have constructed a complete map of how human DNA is mixed as it is passed down during ...

Complete recombination map of the human genome, a major step in geneticsScientists at deCODE genetics/Amgen have constructed ...

July 2025 will mark the 25th anniversary of the UC Santa Cruz Genome Browser, one of the most widely used resources for genomics worldwide. Originally built to allow researchers to explore a single ...

Long read sequencing revealed more genetic information in cases of 42 patients with rare diseases while cutting time and cost of diagnoses.